|Immunofluorescence (IF)||Assay Dependent|
|Immunohistochemistry (Frozen) (IHC (F))||1:50-1:200|
|Immunohistochemistry (Paraffin) (IHC (P))||1:50-1:200|
|Western Blot (WB)||Assay Dependent|
|Immunohistochemistry (Frozen) (IHC (F))||See 2 publications below|
|Immunohistochemistry (IHC)||See 3 publications below|
|Immunofluorescence (IF)||See 3 publications below|
|Miscellaneous PubMed (MISC)||See 3 publications below|
|Western Blot (WB)||See 3 publications below|
|Tested Species reactivity||Human, Mouse|
|Published species reactivity||Mouse|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic peptide derived from the C-terminal region of the mouse Connexin 47 protein.|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7.4|
|Contains||0.1% sodium azide|
36-4700 was used in immunofluorescence analysis of Connexin47 (Cx47) on sections of adult mouse brain.
This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: connexin 47 type A; connexin 47 type C; connexin 47 type D; Connexin-46.6; Connexin-47; Cx46.6; Cx47; Gap junction alpha-12 protein; Gap junction gamma-2 protein; gap junction membrane channel protein alpha 12; gap junction protein, chi 2; gap junction protein, gamma 2, 47kDa; GJA12; GJC2
Gene Aliases: B230382L12Rik; CX46.6; Cx47; GJA12; GJC2; HLD2; LMPH1C; PMLDAR; SPG44
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